APPLICATION SITE SCAR side effect
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Drugs associated with APPLICATION SITE SCAR
ABREVA BENADRYL CATAPRES CLIMARA DURAGESIC EMSAM ESTRADERM NEUPRO NICOTINE NIZORALEmsam Side Effects Report #5546032-1
Physician from UNITED STATES reported EMSAM problem on Oct 19, 2007. Female patient, 57 years of age, weighting 198.4 lb, was diagnosed with major depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site scar, hypertrichosis, rash, . EMSAM dosage: unknown. During the same period patient was treated with OXYCONTIN, AMBIEN CR, JANUVIA, OXYCODONE, KLONOPIN, ZANAFLEX, SYNTHROID, ZYRTEC. Patient recovered.
Emsam Side Effects Report #5448882-9
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 13, 2007. Female patient, 57 years of age, weighting 198.4 lb, was diagnosed with depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site scar, hypertrichosis, rash, . EMSAM dosage: unknown. During the same period patient was treated with OXYCONTIN, AMBIEN CR, JANUVIA, OXYCODONE, KLONOPIN, ZANAFLEX, SYNTHROID, ZYRTEC. Patient recovered.
Abreva Side Effects Report #5461701-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Dec 04, 2006. Female patient, 45 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462241-4
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 34 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462256-6
Consumer or non-health professional from UNITED STATES reported ABREVA problem on June 06, 2007. Female patient, 49 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462651-5
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Female patient, 29 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462804-6
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 15, 2007. Female patient, 27 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462832-0
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 23, 2007. Female patient, 37 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, . ABREVA dosage: unknown. Patient recovered.
Estraderm Side Effects Report #5420478-4
Consumer or non-health professional from UNITED KINGDOM reported ESTRADERM problem on Aug 16, 2007. Female patient, 49 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site scar, application site vesicles, urticaria, . ESTRADERM dosage: 50MG DAILY. Patient recovered.
Estraderm Side Effects Report #5381630-X
ESTRADERM problem was reported by a Pharmacist from UNITED KINGDOM on June 28, 2007. Female patient, 49 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site scar, application site vesicles, urticaria, . ESTRADERM dosage: 50MG DAILY. Patient recovered.
Estraderm Side Effects Report #5388960-6
Consumer or non-health professional from UNITED KINGDOM reported ESTRADERM problem on July 10, 2007. Female patient, 49 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site scar, application site vesicles, urticaria, . ESTRADERM dosage: 50MG DAILY. Patient recovered.
Estraderm Side Effects Report #5381630-X
ESTRADERM problem was reported by a Pharmacist from UNITED KINGDOM on June 28, 2007. Female patient, 49 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site scar, application site vesicles, urticaria, . ESTRADERM dosage: 50MG DAILY. Patient recovered.
Estraderm Side Effects Report #5388960-6
Consumer or non-health professional from UNITED KINGDOM reported ESTRADERM problem on July 10, 2007. Female patient, 49 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site scar, application site vesicles, urticaria, . ESTRADERM dosage: 50MG DAILY. Patient recovered.
Nizoral Side Effects Report #5747978-1
NIZORAL problem was reported by a Consumer or non-health professional from AUSTRALIA on May 15, 2008. Male patient, 43 years of age, was diagnosed with fungal skin infection and was treated with NIZORAL. After drug was administered, patient experienced the following problems/side effects: application site scar, blister, burning sensation, skin exfoliation, . NIZORAL dosage: unknown. Patient recovered.
Duragesic Side Effects Report #5750682-7
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on May 19, 2008. Male patient, weighting 148.0 lb, was diagnosed with pain, bladder cancer and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site scar, application site ulcer, blood cholesterol increased, dental caries, depression, pain, speech disorder, tooth loss, . DURAGESIC dosage: unknown. During the same period patient was treated with OXYCODONE, ATENOLOL, ADVAIR DISKUS, URELLE, OMEPRAZOLE. Patient recovered.
Duragesic Side Effects Report #5357189-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on June 06, 2007. Male patient, weighting 148.0 lb, was diagnosed with pain, bladder cancer and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site scar, application site ulcer, blood cholesterol increased, dental caries, depression, pain, speech disorder, tooth loss, . DURAGESIC dosage: unknown. During the same period patient was treated with OXYCODONE, ATENOLOL, ADVAIR DISKUS, URELLE, OMEPRAZOLE. Patient recovered.
Duragesic Side Effects Report #5284145-2
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 06, 2007. Female patient, weighting 169.0 lb, was diagnosed with pain, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site scar, herpes zoster, . DURAGESIC dosage: unknown. During the same period patient was treated with OPANA, OXYCONTIN, OXYCODONE, NORTRIPTYLINE. Patient recovered.
Duragesic Side Effects Report #5296266-9
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2007. Female patient, weighting 169.0 lb, was diagnosed with pain, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site scar, herpes zoster, . DURAGESIC dosage: unknown. During the same period patient was treated with OPANA, OXYCONTIN, OXYCODONE, NORTRIPTYLINE. Patient recovered.
Duragesic Side Effects Report #5645188-X
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 20, 2008. Male patient, weighting 299.0 lb, was diagnosed with pain, breakthrough pain, fluid retention and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site scar, thrombosis, withdrawal syndrome, . DURAGESIC dosage: unknown. During the same period patient was treated with VICODIN, PERCOCET, HYDROCHLOROTHIAZIDE, DEMADEX. Patient was hospitalized. Patient recovered.
Catapres Side Effects Report #5564070-X
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 20, 2007. Female patient, 84 years of age, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site irritation, application site scar, . CATAPRES dosage: unknown. Patient recovered.
Neupro Side Effects Report #5588954-1
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Oct 30, 2007. Female patient, 52 years of age, was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site reaction, application site scar, hallucination, . NEUPRO dosage: unknown. During the same period patient was treated with SINEMET, TASMAR. Patient recovered.
Nicotine Side Effects Report #5515218-4
NICOTINE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Male patient was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site burn, application site scar, blood pressure increased, headache, insomnia, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. Patient recovered.
Abreva Side Effects Report #5462192-5
Consumer or non-health professional from UNITED STATES reported ABREVA problem on May 18, 2007. Female patient, 36 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site dryness, application site scar, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462237-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 25 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site scar, application site swelling, hypersensitivity, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462370-5
Consumer or non-health professional from UNITED STATES reported ABREVA problem on July 09, 2007. Male patient, 53 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site reaction, application site scar, skin depigmentation, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462640-0
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 14, 2007. Female patient, 74 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site scar, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462659-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Feb 20, 2007. Female patient, 59 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scab, application site scar, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Neupro Side Effects Report #5677074-3
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2007. Female patient, 52 years of age, was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site reaction, application site scar, hallucination, . NEUPRO dosage: 2MG/5ML, 1 IN 1 D; 4MG/24H, 1 IN 1 D; 6MG/24H, 1 IN 1 D; 2 MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with SINEMET, TASMAR. Patient recovered.
Benadryl Side Effects Report #5719382-3
Consumer or non-health professional from UNITED STATES reported BENADRYL CREAM EXTRA STRENGTH problem on Apr 17, 2008. Female patient, 47 years of age, weighting 170.0 lb, was diagnosed with rash and was treated with BENADRYL CREAM EXTRA STRENGTH. After drug was administered, patient experienced the following problems/side effects: application site burn, application site scar, . BENADRYL CREAM EXTRA STRENGTH dosage: unknown. Patient recovered.
Duragesic Side Effects Report #5276810-8
DURAGESIC problem was reported by a Physician from UNITED STATES on Mar 21, 2007. Female patient, weighting 164.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site abscess, application site scar, device failure, irritable bowel syndrome, microcytic anaemia, staphylococcal infection, . DURAGESIC dosage: unknown. During the same period patient was treated with VICODIN, TRAZODONE, RISPERDAL, MOBIC, PROTONIX, NEURONTIN. Patient was hospitalized. Patient recovered.
Climara Side Effects Report #5508074-1
Consumer or non-health professional from UNITED STATES reported CLIMARA PRO problem on Nov 01, 2007. Female patient, 60 years of age, weighting 149.9 lb, was treated with CLIMARA PRO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site scar, cervical polyp, metrorrhagia, . CLIMARA PRO dosage: 0.045 / 0.015 MG/D, CONT. During the same period patient was treated with CLIMARA PRO, CALCIUM, ASCORBIC ACID, FOLIC ACID. Patient recovered.
Abreva Side Effects Report #5462240-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 76 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site scar, . ABREVA dosage: unknown. Patient recovered.
Abreva Side Effects Report #5462851-4
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 27, 2007. Female patient, 41 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site discolouration, application site irritation, application site scar, hypersensitivity, hypoaesthesia oral, oral herpes, . ABREVA dosage: unknown. Patient recovered.
Duragesic Side Effects Report #5734713-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2008. Female patient, weighting 130.0 lb, was diagnosed with back pain, sleep disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: anxiety, application site scab, application site scar, eczema, pancreatitis acute, . DURAGESIC dosage: unknown. During the same period patient was treated with AMITRIPTLINE. Patient was hospitalized. Patient recovered.